Canonical Allele Identifier: CA2676178098
Gene: SGCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156508668_156508670dup , CM000667.2:g.156508668_156508670dup GRCh38
NC_000005.9:g.155935678_155935680dup , CM000667.1:g.155935678_155935680dup GRCh37
NC_000005.8:g.155868256_155868258dup NCBI36
NG_008693.2:g.643325_643327dup , LRG_205:g.643325_643327dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.260_262dup MANE Select ENSP00000338343.4:p.Gln87_Pro88insGln
ENST00000337851.8:c.260_262dup ENSP00000338343.4:p.Gln87_Pro88insGln
ENST00000435422.7:c.257_259dup ENSP00000403003.2:p.Gln86_Pro87insGln
ENST00000517913.5:c.260_262dup ENSP00000429378.1:p.Gln87_Pro88insGln
ENST00000524347.2:c.*124_*126dup ENSP00000430794.1:n.*124_*126dup
NM_000337.5:c.260_262dup , LRG_205t1:c.260_262dup NP_000328.2:p.Gln87_Pro88insGln
NM_001128209.1:c.257_259dup NP_001121681.1:p.Gln86_Pro87insGln
NM_172244.2:c.260_262dup NP_758447.1:p.Gln87_Pro88insGln
XM_005265966.3:c.260_262dup XP_005266023.1:p.Gln87_Pro88insGln
XM_005265967.1:c.260_262dup XP_005266024.1:p.Gln87_Pro88insGln
XM_006714911.2:c.260_262dup XP_006714974.1:p.Gln87_Pro88insGln
XM_011534621.1:c.257_259dup XP_011532923.1:p.Gln86_Pro87insGln
XM_005265966.5:c.260_262dup XP_005266023.1:p.Gln87_Pro88insGln
XM_005265967.2:c.260_262dup XP_005266024.1:p.Gln87_Pro88insGln
XM_011534621.2:c.257_259dup XP_011532923.1:p.Gln86_Pro87insGln
XM_017009723.2:c.260_262dup XP_016865212.1:p.Gln87_Pro88insGln
XM_017009724.1:c.260_262dup XP_016865213.1:p.Gln87_Pro88insGln
NM_001128209.2:c.257_259dup NP_001121681.1:p.Gln86_Pro87insGln
NM_172244.3:c.260_262dup NP_758447.1:p.Gln87_Pro88insGln
NM_000337.6:c.260_262dup MANE Select NP_000328.2:p.Gln87_Pro88insGln